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Filaggrin Polymorphisms and the Uptake of Chemicals through the Skin—A Human Experimental Study

Filaggrin Polymorphisms and the Uptake of Chemicals through the Skin—A Human Experimental Study

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_swepub_ki_se_465191

Filaggrin Polymorphisms and the Uptake of Chemicals through the Skin—A Human Experimental Study

Publication information

Publisher

United States: National Institute of Environmental Health Sciences

More information

Scope and Contents

Contents

The filaggrin protein is important for skin barrier structure and function. Loss-of-function (null) mutations in the filaggrin gene
may increase dermal absorption of chemicals.
The objective of the study was to clarify if dermal absorption of chemicals differs depending on
genotype.
We performed a quantitative real-time polymerase chain reaction (qPCR)-based genetic screen for loss-of-function mutations (
null) in 432 volunteers from the general population in southern Sweden and identified 28
null carriers. In a dermal exposure experiment, we exposed 23
null and 31 wild-type (wt) carriers to three organic compounds common in the environment: the polycyclic aromatic hydrocarbon pyrene, the pesticide pyrimethanil, and the ultraviolet-light absorber oxybenzone. We then used liquid-chromatography mass-spectrometry to measure the concentrations of these chemicals or their metabolites in the subjects' urine over 48 h following exposure. Furthermore, we used long-range PCR to measure
repeat copy number variants (CNV), and we performed population toxicokinetic analysis.
Lag times for the uptake and dermal absorption rate of the chemicals differed significantly between
null and wt carriers with low (20-22 repeats) and high
CNV (23-24 repeats). We found a dose-dependent effect on chemical absorption with increasing lag times by increasing CNV for both pyrimethanil and pyrene, and decreasing area under the urinary excretion rate curve (
) with increasing CNV for pyrimethanil.
null carriers excreted 18% and 110% more metabolite (estimated by
) for pyrimethanil than wt carriers with low and high CNV, respectively.
We conclude that
genotype influences the dermal absorption of some common chemicals. Overall,
null carriers were the most susceptible, with the shortest lag time and highest rate constants for skin absorption, and higher fractions of the applied dose excreted. Furthermore, our results indicate that low
CNV resulted in increased dermal absorption of chemicals. https://doi.org/10.1289/EHP7310....

Alternative Titles

Full title

Filaggrin Polymorphisms and the Uptake of Chemicals through the Skin—A Human Experimental Study

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_swepub_primary_oai_swepub_ki_se_465191

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_swepub_ki_se_465191

Other Identifiers

ISSN

0091-6765

E-ISSN

1552-9924

DOI

10.1289/EHP7310

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